Seeking confidence in the diagnosis of systemic AL (Ig light-chain) amyloidosis: patients can have both monoclonal gammopathies and hereditary amyloid proteins.

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Published in Blood on January 26, 2006

Authors

Raymond L Comenzo1, Ping Zhou, Martin Fleisher, Bradly Clark, Julie Teruya-Feldstein

Author Affiliations

1: Howard 802, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY 10021, USA. comenzor@mskcc.org

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